TAPT1 encodes a highly conserved protein that localizes to the centrosome and/or ciliary basal body. Mutations in TAPT1 disrupt Golgi morphology and trafficking and normal primary cilium formation and these mutations are congenitally manifested by severe undermineralization of the intra-uterine skeleton. A mutation in the mouse ortholog of TAPT1 results in homeotic, posterior-to-anterior transformations of the axial skeleton which are similar to the phenotype of mouse homeobox C8 gene mutants. In mouse, TAPT1 is thought to function downstream of homeobox C8 to transduce extracellular patterning information during axial skeleton development.
Chicken Transmembrane anterior posterior transformation protein 1 homolog (TAPT1) ELISA Kit employs a two-site sandwich ELISA to quantitate TAPT1 in samples. An antibody specific for TAPT1 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyTAPT1 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for TAPT1 is added to the wells. After washing, Streptavidin conjugated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of TAPT1 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Chicken Transmembrane anterior posterior transformation protein 1 homolog (TAPT1) ELISA Kit listed herein is for research use only and is not intended for use in human or clinical diagnosis. Suggested applications of our products are not recommendations to use our products in violation of any patent or as a license. We cannot be responsible for patent infringements or other violations that may occur with the use of this product.
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